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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41721Generated: October 24, 2026

Water → (e)-3-[3'-Adamantan-1-yl-4'-(2-methoxyethoxymethoxy)-biphenyl-4-yl]-acrylic acid methyl ester

https://huagongshe.com/en/reaction/41721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant1-(Chloromethoxy)-2-methoxyethaneHCID 77590—
Reactant(E)-3-(3'-adamantan-1-yl-4'-hydroxybiphenyl-4-yl)-acrylic acid methyl esterHCID 10293655—
SolventDimethylformamideHCID 6228—
Product(e)-3-[3'-Adamantan-1-yl-4'-(2-methoxyethoxymethoxy)-biphenyl-4-yl]-acrylic acid methyl esterHCID 6740151384%

Reaction Steps

A solution of (E)-3-(3′-adamantan-1-yl-4′-hydroxybiphenyl-4-yl)-acrylic acid methyl ester (120 mg, 0.309 mmol) in 1 ml of anhydrous DMF, was dropped into a 1 ml suspension of NaH (14.8 mg, 0.371 mmol, 60% in mineral oil) in anhydrous DMF (0.3 ml) at 0° C. The resulting red solution was stirred at RT for 30 min, then MEM-Cl (46 mg, 0.371 mmol) was added. After stirring overnight at RT, iced water was added and the mixture was extracted several times with EtOAc. The combined organic phases were dried over Na2SO4, filtered and concentrated under vacuo. The resulting crude product was purified on silica gel (acetone:hexane 15:85) to obtain (E)-3-[3′-adamantan-1-yl-4′-(2-methoxyethoxymethoxy)-biphenyl-4-yl]-acrylic acid methyl ester (123 mg, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530517B2
Source datasetuspto-grants-2013_09
ORD IDord-f9cf0256f72f44759f3049c41035d6eb
Source noteuspto-grants-2013_09